Spang A, Courtney I, Grein K, Matzner M, Schiebel E
Max-Planck-Institut für Biochemie, Genzentrum, Martinsried, Germany.
J Cell Biol. 1995 Mar;128(5):863-77. doi: 10.1083/jcb.128.5.863.
KAR1 has been identified as an essential gene which is involved in karyogamy of mating yeast cells and in spindle pole body duplication of mitotic cells (Rose, M. D., and G. R. Fink. 1987. Cell. 48:1047-1060). We investigated the cell cycle-dependent localization of the Kar1 protein (Kar1p) and its interaction with other SPB components. Kar1p is associated with the spindle pole body during the entire cell cycle of yeast. Immunoelectron microscopic studies with anti-Kar1p antibodies or with the monoclonal antibody 12CA5 using an epitope-tagged, functional Kar1p revealed that Kar1p is associated with the half bridge or the bridge of the spindle pole body. Cdc31p, a Ca(2+)-binding protein, was previously identified as the first component of the half bridge of the spindle pole body (Spang, A., I. Courtney, U. Fackler, M. Matzner, and E. Schiebel. 1993. J. Cell Biol. 123:405-416). Using an in vitro assay we demonstrate that Cdc31p specifically interacts with a short sequence within the carboxyl terminal half of Kar1p. The potential Cdc31p-binding sequence of Kar1p contains three acidic amino acids which are not found in calmodulin-binding peptides, explaining the different substrate specificities of Cdc31p and calmodulin. Cdc31p was also able to bind to the carboxy terminus of Nuflp/Spc110p, another component of the SPB (Kilmartin, J. V., S. L. Dyos, D. Kershaw, and J. T. Finch. 1993. J. Cell Biol. 123:1175-1184). The association of Kar1p with the spindle pole body was independent of Cdc31p. Cdc31p, on the other hand, was not associated with SPBs of kar1 cells.
KAR1已被鉴定为一个必需基因,它参与交配酵母细胞的核融合以及有丝分裂细胞的纺锤极体复制(罗斯,M.D.,和G.R.芬克。1987年。《细胞》。48:1047 - 1060)。我们研究了Kar1蛋白(Kar1p)在细胞周期中的定位及其与其他纺锤极体成分的相互作用。在酵母的整个细胞周期中,Kar1p都与纺锤极体相关联。使用抗Kar1p抗体或单克隆抗体12CA5对带有表位标签的功能性Kar1p进行免疫电子显微镜研究表明,Kar1p与纺锤极体的半桥或桥相关联。Cdc31p是一种钙结合蛋白,先前被鉴定为纺锤极体半桥的第一个成分(斯潘,A.,I.考特尼,U.法克勒,M.马茨纳,和E.施贝尔。1993年。《细胞生物学杂志》。123:405 - 416)。通过体外试验,我们证明Cdc31p与Kar1p羧基末端一半内的一个短序列特异性相互作用。Kar1p的潜在Cdc31p结合序列包含三个酸性氨基酸,这些氨基酸在钙调蛋白结合肽中未发现,这解释了Cdc31p和钙调蛋白不同的底物特异性。Cdc31p也能够结合到纺锤极体的另一个成分Nuflp/Spc110p的羧基末端(基尔马丁,J.V.,S.L.迪奥斯,D.克肖,和J.T.芬奇。1993年。《细胞生物学杂志》。123:1175 - 1184)。Kar1p与纺锤极体的关联不依赖于Cdc31p。另一方面,Cdc31p不与kar1细胞的纺锤极体相关联。